Job Description

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Your responsibilities will include

Redaction of clinical trial documents and anonymisation of individual patient data Preparing redaction proposal document packages for EMA Policy 0070 and Health Canada PRCI submissions Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Disclosure activities for drug and device clinical trial information:
+ Authoring of protocol registrations and results postings for submission to local and global regulatory agencies
+ Maintenance of study records including status tracking and administrative aspects
Managing timelines for timely submission to ensure compliance with international laws, regulations, and guidelines Communicate and coordinate with international study teams, act as a central point of contact
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Your profile

University degree in data science or life science related discipline Knowledge of drug development and clinical science Experience in redaction of CCI and PPD in clinical documents is a plus Knowledge of EMA policy 0070 and Health Canada PRCI is a plus Experience in data anonymization and programming (e.g., R/SAS) is a plus Knowledge of the clinical trials disclosure regulatory environment and experience with Clinicaltrials.gov and EudraCT/CTIS is a plus Experience in medical writing is a plus Fast comprehension, analytical thinking, teamwork and a high degree of initiative, willingness to learn Work experience in a CRO or pharma/biotech is a plus Excellent organizational and time management skills, highly detail-oriented Good English skills, German is an advantage
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What we offer you

We value communication, flat hierarchies, open corporate culture, and a harmonious work environment. We offer comprehensive individual development opportunities, continuous trainings, and flexible working hours. A modern and bright office with a subsidised canteen, as well as the opportunity to work 2 days per week from home are part of our everyday working life. Full remote work from anywhere in Germany for those who do not live in Munich can be discussed. You will join an interdisciplinary team allowing you to discuss with and learn from peers with many different backgrounds.

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Question?

If you have any questions, please feel free to contact us by e-mail application@staburo.de.

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About us

Staburo GmbH is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our core competencies include Clinical Statistics, Translational Medicine & Biomarkers, Phase I & Pharmacokinetics/-Dynamics, Data Transparency & Disclosure Services, Health Technology Assessment and Bioinformatics. Our customers are international pharmaceutical companies, CROs, biotech companies and medical device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results.